A synthesis of a thysanone analog

被引：16

作者：

Kraus, GA ^{[1
]}

Ogutu, H ^{[1
]}

机构：

[1] Iowa State Univ Sci & Technol, Dept Chem, Ames, IA 50011 USA

来源：

TETRAHEDRON | 2002年 / 58卷 / 37期

基金：

美国国家卫生研究院;

关键词：

thysanone analog; hemiacetal; chemotherapeutic agents;

D O I：

10.1016/S0040-4020(02)00823-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Hemiacetal 10 was prepared in 13 steps from dimethoxybenzaldehyde. Key steps included the salcomine oxidation of a phenol and a selective deprotection using boron trichloride. (C) 2002 Elsevier Science Ltd. All rights reserved.

引用

页码：7391 / 7395

页数：5

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